Bandim Health Project, Indepth Network, Apartado 861, Bissau 1004, Guinea-Bissau.
Institute of Health, Aarhus University, Nordre Ringgade 1, Aarhus C 8000, Denmark.
Trans R Soc Trop Med Hyg. 2020 Aug 1;114(8):566-574. doi: 10.1093/trstmh/traa023.
Manual white blood cell (WBC) differential counts as a predictor for neonatal sepsis development in a low-resource setting have not been thoroughly evaluated. We hypothesized that manual differentiation (specifically immature:total [I:T] neutrophil ratios) would be feasible and useful as an adjunct to predict early-onset neonatal sepsis (EONS). Secondarily, we hypothesized that vaccination with bacillus Calmette-Guérin (BCG) and oral polio vaccine (OPV) could alter WBC differential counts and thus might reduce its predictive performance.
We performed a prospective cohort study within a randomized trial, randomizing healthy, high-risk newborns admitted to the nursery at the national hospital in Guinea-Bissau 1:1 to BCG+OPV at admission or at discharge (usual practice). Thin capillary blood films were prepared at 2 d of age in a subset of 268 neonates. WBC counts were assessed by microscopy and neonates were followed up for sepsis development within 2 weeks.
Ninety-eight percent (264/268) of smears provided interpretable reads. Of the 264 children, 136 had been randomized to receive BCG+OPV prior to sampling; the remaining 128 were vaccinated at discharge. The I:T ratio (average 0.017) was lower among children who did not develop clinical sepsis but did not predict sepsis (p=0.70). Only three children had an I:T ratio >0.2 (associated with a higher probability of clinical sepsis in previous studies) but did not develop sepsis. Immunization did not alter WBC composition.
Manual WBC differentials are feasible in low-resource settings. WBC differentials are not affected by standard newborn immunization. However, the I:T ratio had no value in predicting subsequent development of sepsis.
手动白细胞(WBC)分类计数作为预测资源匮乏环境中新生儿败血症发展的指标尚未得到充分评估。我们假设手动区分(特别是不成熟:总[I:T]中性粒细胞比)是可行且有用的,可以作为预测早发性新生儿败血症(EONS)的辅助手段。其次,我们假设卡介苗(BCG)和口服脊髓灰质炎疫苗(OPV)的接种可能会改变 WBC 分类计数,从而降低其预测性能。
我们在几内亚比绍国家医院的新生儿病房进行了一项前瞻性队列研究,在一项随机试验中,将 268 名高危新生儿以 1:1 的比例随机分为入院时或出院时(常规做法)接种 BCG+OPV。在 268 名新生儿中,有 264 名新生儿在 2 天龄时采集了薄毛细血管血涂片。通过显微镜评估 WBC 计数,并在 2 周内对新生儿进行败血症发展的随访。
98%(264/268)的涂片提供了可解释的读数。在 264 名儿童中,有 136 名在接受采样前被随机分配接受 BCG+OPV;其余 128 名在出院时接种疫苗。未发生临床败血症但未预测败血症的儿童的 I:T 比值(平均 0.017)较低,但未发生败血症(p=0.70)。只有 3 名儿童的 I:T 比值>0.2(与以前的研究中临床败血症的可能性较高相关),但没有发生败血症。免疫接种并未改变 WBC 组成。
在资源匮乏的环境中,手动 WBC 分类是可行的。WBC 分类不受标准新生儿免疫接种的影响。然而,I:T 比值在预测随后发生败血症方面没有价值。